Abstract: An additive for synthetic resins includes a [liquid rubber]/[polyester] block copolymer comprising block liquid rubber compound parts and block polyester parts as constituent segments. One or more of these polyester blocks are connected to each one of the polydiene block parts through ester bond.

Abstract: An additive for synthetic resins contains a block copolymer having as its constituent segments both polyester block obtainable by ring-opening polymerization of .epsilon.-aliphatic lactone and polydiene block. One or more of these polyester blocks are connected to the polydiene block through ester bond and at least one of these polyester blocks has at its end a reactive group such as vinyl group, epoxy group, isocyanate group or carboxyl group.

Abstract: The invention relates to a polymer having the structure ##STR1## and mixtures thereof wherein R is a perhalogenated aromatic or cyclo aliphatic radical containing from 6 to 7 carbon atoms in the cyclic structure; R.sup.1 is hydroxy or C.sub.1 to C.sub.10 alkoxy; R.sup.2 is hydrogen or C.sub.1 to C.sub.10 alkyl; EO represents the radical --CH.sub.2 CH.sub.2 O--; PO represents the radical ##STR2## m is an integer having a value of from 6 to 20; and x, y, z, x', y' and z' each represent an integer having a value of from 0 to 50 with the proviso that the sums of x+y+z and of x'+y'+z' are greater than 5.The application is also directed to the preparation and use of the above polymer.

Abstract: Disclosed is a process for the co-production of aromatic carboxylic esters and alkyl iodides by the carbonylation of aromatic iodides in the presence of an alkanol and a palladium catalyst.

Abstract: The present invention is directed to a polyester polyol having a molecular weight between about 850 and 2000, a functionality of about 5 to 9 and an OH number of about 200 to 350, based on 100% solids, which is prepared by reacting(a) an acid component based on at least one polyfunctional cycloaliphatic or aromatic carboxylic acid, anhydride or ester and optionally up to about 50 percent by weight of at least one acyclic, polyfunctional carboxylic acid and(b) a hydroxyl component containing at least a portion of at least one polyol having a functionality of at least 3.The present invention is also directed to a process for preparing these polyester polyols by reacting the above components and is further directed to the use of these polyester polyols in combination with organic polyisocyanates for the production of polyurethanes, particularly polyurethane coatings.

Abstract: There are described vinyl ether terminated ester oligomers which cure or polymerize particularly rapidly, especially by cationic polymerization which is radiation induced in the presence of an onium salt. The oligomeric units arise from the reaction of a polycarboxylic acid having at least three carboxylic acid groups with a diol, although esters with triols and higher polyhydric diols also are useful, especially where an extensively cross-linked product is desired. The carboxyl-terminated oligomeric esters are esterfied with vinyl ether terminated alcohols which can be thought of as the adducts of alkynes and diols.

Abstract: A process for the preparation of polyester polyols having an acid number of less than 1, a hydroxyl number of approximately 20 to about 400, and having a functionality of efficaciously 2 to 3, wherein polycarboxylic acids and/or their anhydrides and multivalent alcohols are polycondensed, preferably in the absence of common esterification catalysts, at temperatures of from about 150.degree. to 250.degree. C., optionally under reduced pressure, up to an acid number of from 20 to 5. The resulting polycondensate is then oxyalkylated per carboxyl group using from 1 to 5 moles of an alkylene oxide, for example 1,2-propylene oxide and/or preferably ethylene oxide, in the presence of at least one tertiary amine catalyst from the group consisting of N-methylimidazole, diazabicyclo[2,2,2]octane, diazabicyclo[5,4,0]undec-7-ene and pentamethyldiethylenetriamine and mixtures thereof, in a quantity of from about 0.001 to 1.0 weight percent based on the weight of the polycondensate, at temperatures from about 100.degree.

Abstract: Metabolically-acceptable, surgical adhesives are prepared from polyisocyanates having the structral formula: ##STR1## wherein R is a polyvalent aliphatic radical of about 1 to 10 carbon atoms or a polyvalent aromatic radical of 6 to about 24 carbon atoms;A is C, S or P;Z is O or S;Y is 1 when A is C or P, and 2 when A is S;n is 1 or 2;p is at least 1;q is 0 or 1, with the proviso that when A is carbon or sulfur, q is 0;r is 0 or 1, with the proviso that when A is carbon or sulfur, r is 0;X is a residue of an organic compound having active hydrogen-containing groups; andX' is a residue of an organic compound having at least 1 active hydrogen-containing group.

Abstract: The invention relates to a polymer having the structure ##STR1## and mixtures thereof wherein R is a perhalogenated aromatic or cyclo aliphatic radical containing from 6 to 7 carbon atoms in the cyclic structure; R.sup.1 is hydroxy or C.sub.1 to C.sub.10 alkoxy; R.sup.2 is hydrogen or C.sub.1 to C.sub.10 alkyl; EO represents the radical --CH.sub.2 CH.sub.2 O--; PO represents the radical ##STR2## m is an integer having a value of from 6 to 20; and x, y, z, x', y' and z' each represent an integer having a value of from 0 to 50 with the proviso that the sums of x+y+z and of x'+y'+x' are greater than 5.The application is also directed to the preparation and use of the above polymer.

Abstract: A polyester polyol having the idealized structure: ##STR1## where R represents the residue of a polyepoxide after ring opening with a carboxylic acid group, R' represents the residue of a cyclic anhydride, n is a number of from 4 to 25, m represents the number of epoxy groups of the polyepoxide ring opened with carboxylic acid groups, and R" represents --H or --CH.sub.3.

Abstract: Oligoesters having hydroxyl groups and an OH number of from 200 to 600 mg KOH/g are made by reacting a cyclic dicarboxylic acid anhydride in which no halogen is present with a polyfunctional alcohol or dialkanolamine in a molar ratio of from 1:0.5 to 1:1.5 at a temperature of from 50.degree. to 150.degree. C. to form the corresponding dicarboxylic acid semiester and/or semiamide. This semiester and/or semiamide is then alkoxylated with ethylene oxide and/or propylene oxide in the presence of a catalyst at 80.degree. to 150.degree. C. The equivalent ratio of acid groups to alkylene oxide groups is from 1:0.8 to 1:1.7. The catalysts are reaction products of alkoxides with at least 3 C-atoms with ammonia, piperidine, piperazine and/or C.sub.2 -C.sub.6 aliphatic, polyamines, preferably diamines in which all of the NH-functional groups have been alkoxylated. The resultant oligoester may then be reacted with a polyisocyanate optionally in the presence of known additives, such as blowing agents and catalysts.

Abstract: A polyester polyol suitable for use in a foam-forming reaction with an organic polyisocyanate in the manufacture of a polyurethane or polyisocyanurate foam, the polyester polyol being the reaction product of polycarboxylic acid and polyol components, wherein the polyol component solely or partially comprises an oxyalkylated polyol selected from the group consisting of(a) at least one oxyalkylated polyol having at least one primary and at least one secondary hydroxyl group, and(b) an oxyalkylated polyol mixture containing at least one oxyalkylated polyol having at least one primary and at least one secondary hydroxyl group.

Abstract: There are described vinyl ether terminated ester oligomers which cure or polymerize particularly rapidly, especially by cationic polymerization which is radiation induced in the presence of an onium salt. The oligomeric units arise most often from the reaction of a dicarboxylic acid with a diol, although esters with triols and higher polyhydric polyols also are useful, especially where an extensively cross-linked product is desired. The carboxyl-terminated oligomeric esters are esterified with vinyl ether terminated alcohols which can be thought of as the adducts of alkynes and polyols, especially diols.

Abstract: A process for preparation of a purified bis(2-hydroxyethyl) ester of 2,6-naphthalenedicarboxylic acid wherein 2,6-naphthalenedicarboxylic acid is reacted with a catalyst comprised of a tertiary amine and a titanium-containing compound in order to produce the ester.

Abstract: Fluorocarbon blowing agent compatible polyol blends are provided comprising reaction products of a combination of (a) a residue from the manufacture of dimethyl terephthalate, (b) a low molecular weight diol compound, (c) a nonionic surfactant compound, (d) optionally a hydrophobic compound, and (e) optionally a polybasic carboxylic acid compound. These polyol blends are produced by a simple heating process and are thereafter optionally blendable with various conventional polyols and other additives (including fluorocarbons and catalysts) to make resin prepolymer blends. Such resin blends can be catalytically reacted with organic isocyanates to produce cellular polyurethanes and polyurethane/polyisocyanurates.

Abstract: Disclosed is a mixture of terephthalic acid ester polyols for use in the preparation of rigid polyurethane and polyisocyanurate foams. The polyols are prepared by reacting scrap polyethylene terephthalate, dimethyl terephthalate process residue and an excess of a mixture of glycols.

Abstract: Block polyesters having branched hydrophilic capping groups which are useful as soil release agents in detergent compositions are disclosed. Preferred polyesters have the formula; ##STR1## wherein each R.sup.1 is a 1,4-phenylene moiety; the R.sup.2 are essentially ethylene moieties, 1,2-propylene moieties or a mixture thereof; each X is ethyl or preferably methyl; each n.sub.1 is from 1 to about 5; the sum of each n.sub.1 +n.sub.2 is from about 12 to about 43; u is from about 3 to about 10.

Abstract: Capped 1,2-propylene terephthalate-polyoxyethylene terephthalate polyesters useful as soil release agents are disclosed. Preferred polyesters have the formula: ##STR1## wherein each R.sup.1 is a 1,4-phenylene moiety; the R.sup.2 are essentially 1,2-propylene moieties; the R.sup.3 are essentially the polyoxyethylene moiety--(CH.sub.2 CH.sub.2 O).sub.q --CH.sub.2 CH.sub.2 --; each X is ethyl or preferably methyl; each n is from about 12 to about 45; q is from about 12 to about 90; the average value of u is from about 5 to about 20; the average value of v is from about 1 to about 10; the average value of u+v is from about 6 to about 30; the ratio u to v is from about 1 to about 6.

Abstract: Block polyesters useful as soil release agents in detergent compositions are disclosed. Preferred polyesters have the formula: ##STR1## wherein each R.sup.1 is a 1,4-phenylene moiety; the R.sup.2 consist essentially of ethylene moieties, 1,2-propylene moieties or a mixture thereof; each X is ethyl or preferably methyl; each n is from about 12 to about 43; u is from about 3 to about 10.

Abstract: A method for preparing aromatic polyols useful for the production of polyurethane and polyisocyanurate polymers involves digesting scrap polyalkylene terephthalate polymers with a digesting agent, typically a low molecular weight polyol. The digestion product is then treated with an alkylene oxide to produce a low viscosity polyol which displays excellent stability over long term storage.

Abstract: The invention provides a process for the preparation of a polyester oligomer capable of being further polymerized to a high polymer wherein a glycol-dicarboxylic acid ester feed is treated in a secondary esterification zone under conditions such that the partial vapor pressures of water and glycol are maintained at a cumulative level of less than 740 Torr, with water and glycol vapors being continuously removed from the secondary esterification zone, and free glycol being added to the secondary esterification zone in an amount sufficient to maintain a stable amount of liquid glycol in the secondary esterification zone.

Abstract: A novel method for producing a composite ester from dibasic acid, diol and monovalent alcohol through a dehydrating esterification reaction in the first step and then alcohol removing ester interchange reaction in the second step.

Abstract: Novel diimide diacids and modified polyetherimide esters are prepared therefrom by reacting diols, dicarboxylic acids and a combination of the novel diimide diacid and dimer acid. These compositions have many excellent properties which make them particularly useful for extrusion and molding applications.

Abstract: A polyester polyol mixture is prepared by reacting a polycarboxylic acid component-containing polyol with a terephthalic acid residue, wherein the polycarboxylic acid component has ring units with two ##STR1## groups on adjacent or alternate ring positions, the ring unit content of the polycarboxylic acid component being sufficient for viscosity reduction of the polyester polyol mixture. The polyester polyol mixture is useful in the preparation of cellular foam materials, particularly polyisocyanurate and polyurethane foams, and laminates thereof.

Abstract: A new and highly useful resin prepolymer blend of (a) polyester polyols prepared by esterifying phthalic anhydride bottoms with aliphatic polyols; (b) aliphatic polyol, (c) compatibilizing polyalkoxylated compound, and (d) (optionally) polyalkoxylated amine or amide diol. This blend can be reacted with organic isocyanates in the presence of fluorocarbon blowing agent and preferably catalysts to produce cellular polymeric structures.

Abstract: Rigid polyurethane and polyisocyanurate foams are prepared by reacting an excess of an organic polyisocyanate with an etherified modified aromatic polyol. The etherified modified aromatic polyol is prepared by digesting scrap polyalkylene terephthalate polymers with a low molecular weight polyol. The digested polyol is reacted with a low molecular weight polyhydroxy compound containing from about 3 to about 8 hydroxyl groups to form an intermediate product which is alkoxylated with 1 to 4 mols of ethylene oxide and/or propylene oxide to produce a low viscosity etherified modified aromatic polyol which displays excellent stability over long term storage. The etherified modified aromatic polyol is useful in the manufacture of good quality polyurethane and polyisocyanurate foams having improved properties.

Abstract: Fluorinated esters based on multi-ring anhydride systems are disclosed which have excellent anti-soiling properties, durability and resistance to laundering. The compounds are represented by the formula ##STR1## wherein n is 2 or 3, Q is a linking group such as --CO--, --O--, or (C.sub.a H.sub.2a+2-n --(O.sub.2 C).sub.n, R.sub.f is a fluorinated radical, and R is derived from an epoxide such as ethylene oxide or epichlorohydrin. Also disclosed are polyester and nylon fibers having these compounds incorporated therein, and a process for producing such soil-repellent fibers.

Abstract: A composition containing acid halide functional materials, which are useful in the preparation of nylon block polymers, selected from the group consisting of: ##STR1## wherein, X is a halogen;a is an integer equal to 1, 2 or 3;b is an integer equal to 2 or more;R is a di- or a poly-valent group selected from hydrocarbon groups and hydrocarbon groups containing ether linkages;Z is a segment of: (1) a polyether; (2) a polyester containing polyether polyester hydrocarbon segments, (3) a hydrocarbon; (4) a polysiloxane; or (5) combinations thereof.

Abstract: The present invention provides a process for the preparation of monoesters of dicarboxylic acids by the carbonylation of carboxyphenyl-triarylphosphonium salts. The carboxyphenyl-triarylphosphonium salts are reacted with carbon monoxide and an alcohol in a base reaction medium having a pK.sub.b greater than about 8.

Abstract: In order to prepare polyester or polyetherpolyester polyols, polyols, preferably di- to hexafunctional polyether polyols having hydroxyl numbers from 15 to 250 are esterified with at least one carboxylic acid anhydride, preferably phthalic acid anhydride, in the presence of N-methylimidazole, triethylenediamine, and/or triphenylphosphine as catalysts to form a carboxylic acid half-ester, and said half-ester is then oxyalkylated with at least one alkylene oxide, preferably ethylene oxide, in the presence of N-methylimidazole, triethylenediamine, triphenylphosphine, thiodialkylene glycol, employing a mixture of at least two of the compounds cited as catalysts.

Abstract: A composition containing acyllactam functional materials, which are useful in the preparation of nylon block polymers, selected from the group consisting of: ##STR1## wherein, Q is ##STR2## with Y=C.sub.3 -C.sub.11 alkylene; a is an integer equal to 1, 2 or 3;b is an integer equal to 2 or more;R is a di- or a poly- valent group selected from hydrocarbon groups and hydrocarbon groups containing ether linkages;Z is a segment of: (1) a polyether; (2) a polyester containing polyether or polymeric hydrocarbon segments; (3) a hydrocarbon; (4) a polysiloxane; or (5) combinations thereof.

Abstract: A process for producing an oligoester which comprises:(a) the step of reacting isophthalic acid and propylene oxide in a reaction medium in the presence of a specific catalyst comprising a tetraalkyl ammonium compound to prepare an oligoester, and(b) the step of removing volatile components from the resulting oligoester by heating the oligoester at a temperature of 180.degree.-280.degree. C. is disclosed. The oligoester is used as an intermediate for preparing unsaturated polyesters.

Abstract: Polyether-ester polyols are prepared by reacting a polyether polyol, tetrahydrophthalic anhydride and an alkylene oxide in the presence of a catalyst selected from the group consisting of calcium naphthenate and cobalt naphthenate. These polyols may be used in preparing polyurethane products.

Abstract: Homogenous liquid polyol blend compositions containing (a) certain aliphatic polyols, (b) phthalate diester polyols of said aliphatic polyols, and (c) trimellitate polyols of said aliphatic polyols. Such polyol blend compositions are useful in making homogenous liquid resin prepolymer blends compositions containing, in addition to such a polyol blend, fluorocarbon blowing agent, cell stabilizing surfactant, and urethane and/or isocyanurate catalyst. Such a resin prepolymer blend composition is suitable for reaction with organic isocyanates to produce cellular polyurethane and/or polyisocyanurate polymers.

Abstract: A new and highly useful complex mixture of polyester polyols is prepared by esterifying phthalic anhydride bottoms with aliphatic polyols. This mixture can be reacted with organic isocyanates in the presence of fluorocarbon blowing agent and preferably catalysts to produce cellular polymeric structures.

Abstract: Mixtures of aromatic polyols containing ester functionalities suitable for use as polyol extenders in rigid foams prepared by reacting aromatic carbonyl-containing compounds with an alkylene glycol, the reaction product of which is reacted with recycled polyethylene terephthalate are described. Surprisingly, the process is non-catalytic. These novel polyols may be blended with conventional polyols to yield excellent rigid foams, thus serving as useful polyol extenders.

Abstract: A polyether-ester polyol containing a high primary hydroxyl content is prepared employing low amounts of ethylene oxide. The polyurethane foams prepared from these products display improved physical properties with good air flow.

Abstract: Polyester polyols and/or polyester-polyether polyols are prepared by reacting polyols preferably di- to hexafunctional polyether polyols with hydroxyl numbers of 30 to 200 with at least one carboxylic anhydride, preferably glutaric anhydride, resulting in a carboxylic acid half ester which is subsequently oxyalkylated with at least one alkylene oxide, preferably ethylene oxide in the presence of at least 1 thiodialkylene glycol, preferably thiodiethylene and/or thiodipropylene glycol.

Abstract: This invention relates to novel N-cyano amide compositions and adducts thereof of the formula ##STR1## wherein R is a simple organic moiety or a polymeric adduct with the valence of n and n is 2 or 3. The composition, per se, can be used as a curing agent for epoxy resins to form a thermoset material on heating.

Abstract: Polyether-ester polyols are prepared by reacting a crude polyether polyol, tetrahydrophthalic anhydride and an alkylene oxide. These polyols may be used in preparing polyrethane products.

Abstract: The present invention provides a process for the preparation of low molecular weight polyesters directly from hydroxypivaldehyde. The process comprises reacting dry hydroxypivaldehyde with a diester, a multifunctional ester, a diacid, a polyester, or a mixture thereof at a temperature of about 100.degree. C. to 230.degree. C. in the presence of a transesterification catalyst. Optionally, modifying glycols, triols, or polyols may also be added. Suitable catalysts include tetraisopropyl titanate, dibutyltin oxide, lithium hydroxide, and lithium alkoxide, with tetraisopropyl titanate being especially preferred. The reaction is preferably accomplished in two stages by heating the reaction mixture to about 130.degree. C. for about three hours and subsequently heating the reaction mixture to about 190.degree.-230.degree. C. until the reaction is essentially complete.

Abstract: An improved process for exterifying carboxyaromatics is disclosed wherein an anhydride of a carboxyaromatic, such as pyromellitic dianhydride, is reacted with a fluorinated alcohol and an epoxide to give a mixed ester capable of imparting oil and/or water repellency to textiles. The improvement comprises utilizing the epoxide as the reaction medium to reduce reaction times and waste water treatment requirements.

Abstract: Propylene oxide reaction products, and the salts or quaternization products thereof are provided which are obtained from(a) an at least trihydric aliphatic alcohol of 3 to 10 carbon atoms,(b) 1,2-propylene oxide,(c) an aliphatic dicarboxylic acid of 2 to 10 carbon atoms, an aromatic dicarboxylic acid of 8 to 12 carbon atoms or the anhydrides thereof,and at least one of the following components:(d) an aliphatic diol with a molecular weight of at most 2000,(e) a fatty alcohol containing 12 to 22 carbon atoms,(f) a fatty acid containing 12 to 22 carbon atoms, and(g) an aliphatic monoamine or diamine containing 2 to 12 carbon atoms,of which component (g) is used only at the conclusion and only if component (c) is ethylenically unsaturated.The inventive products are suitable for widely varying uses in textile finishing.

Abstract: Polyoxyalkylene polycarboxylate ester is used for imparting soil release properties to textiles such as all polyester fabric either alone or in combination with other textile chemicals.

Abstract: Described is a process for producing unique reaction products from DMT process residue. In the process of this invention DMT process residue is reacted with an excess of dipropylene glycol to give normally liquid, aromatic polyester polyols which are compatible with Freon 11 blowing agent and with glycerol and hence have outstanding utility in the production of blown polyurethane and polyisocyanurate-polyurethane foams.

Abstract: Hexa(meta-,para-carboxyphenyl)benzene compounds. The esters are useful as plasticizers for polyvinylchloride, heat transfer agents, hydraulic fluids, and insulating oils. The acid is suitable as a cross-linking agent for polymers containing hydroxyl or amine groups.

Abstract: Aqueous dispersions of oil-modified, carboxyl-containing, urethane polymers are prepared by reacting diisocyanates or their isocyanate-terminated prepolymers, with half-esters of hindered diols, especially 2,2,4-trimethyl-1,3-pentanediol, and anhydrides of polycarboxylic acids, preferably aromatic acids having at least three carboxylic groups, especially trimellitic anhydride. The urethane polymers are "oil-modified", i.e., extended with unsaturated fatty acid esterpolyols; and when neutralized with ammonia or amines can be dispersed in water to form especially desirable coating compositions. An organic phosphite may be incorporated in the compositions to control the development of hardness in films made from the aqueous dispersions and thereby avoid the formation of wrinkles in films that are made from the compositions.

Abstract: A method if provided for continuously hydrolyzing urethane foam in a vertically oriented hydrolysis reactor. In a preferred practice, a bed of foam particles is formed in the reactor. Superheated steam is flowed continuously upward through the bed at a temperature and rate such that only the foam particles then adjacent the bottom of the reactor are hydrolyzed and the bulk of the bed is not fluidized. Unreacted steam heats the unhydrolyzed foam. Liquid hydrolysis products are drained as they are formed to prevent hydrolysis-impeding liquid saturation of unhydrolyzed particles.

Abstract: Zwitterionic surfactant compounds are made readily biodegradable in the environment by the inclusion of a biochemically and/or hydrolytically labile chemical linkage located between the cationic and anionic charge centers of the compounds and anywhere from the second to the tenth atom distant from the cationic charge center. The biodegradable linkage is preferably an ester or amide. The alkoxylated zwitterionic surfactants herein exhibit outstanding particulate soil removal performance and are also effective in removing oily soils from fabrics, in addition to being readily biodegradable. Also described are detergent compositions containing the zwitterionic surfactants, and, optionally containing cosurfactants and detergent builders.

Abstract: Polyoxyalkylene polycarboxylate ester is used for imparting soil release properties to textiles such as all polyester fabric either alone or in combination with other textile chemicals.